Target intelligence / Profile preview

Cytomegalovirus-derived peptide–Human Leukocyte Antigen complex (CMV-pMHC) (CMV-pMHC)

Target
CMV-pMHC
Molecular classification
Peptide-MHC complex, Antigen-presenting complex, Receptor
01

Overview

The Cytomegalovirus-derived peptide–Human Leukocyte Antigen (CMV-pMHC) complex is a critical immunological target formed when peptides from the human cytomegalovirus (HCMV), such as those from the pp65 (UL83) or IE1 proteins, are processed and presented on the cell surface by HLA class I molecules. This complex is specifically recognized by the T-cell receptors (TCRs) of CD8+ cytotoxic T lymphocytes, which is the primary mechanism for controlling CMV infection in healthy individuals. In immunocompromised patients, such as those undergoing hematopoietic stem cell or solid organ transplantation, the absence of a robust T-cell response against these complexes can lead to viral reactivation, causing significant morbidity and mortality. Therapeutic interventions targeting the CMV-pMHC complex include the adoptive transfer of CMV-specific T cells, TCR-engineered T cells, and the development of TCR-like antibodies or bispecific T-cell engagers that can specifically bind the complex and redirect immune effector cells to kill infected targets. These therapies aim to restore or bypass the host's impaired immune surveillance to eliminate the viral reservoir. However, the high degree of HLA polymorphism restricts specific therapies to certain patient populations, and the risk of off-target cross-reactivity with similar self-peptides remains a significant safety concern. Additionally, CMV has evolved mechanisms to downregulate HLA expression, which can hinder the efficacy of these targeted approaches.

Other names
CMV-HLA complexCMV peptide-MHC complexHCMV-pMHCCMV-pHLA complexCytomegalovirus peptide-major histocompatibility complex
02

Mechanism of action

Recognition by T-cell receptors (TCRs) or TCR-like antibodies, leading to the activation of cytotoxic T lymphocytes (CTLs) and subsequent lysis of CMV-infected cells.

03

Biological functions

Antigen presentationImmune responseT-cell activationViral immune evasion
04

Disease associations

InfectionPost-transplant complicationsCongenital infection
05

Safety considerations

Off-target toxicity (cross-reactivity with self-peptides)Cytokine release syndrome (CRS)HLA downregulation by viral proteinsHLA restriction (limited patient population)
06

Interacting drugs

CMV-specific T cells

3 more in the full profile.

07

Biomarkers

HLA-A*02:01 genotypeCMV serostatusCMV DNA/viral loadCMV-specific T-cell frequency

Beyond the preview

Go deeper on Cytomegalovirus-derived peptide–Human Leukocyte Antigen complex (CMV-pMHC) (CMV-pMHC).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Cytomegalovirus-derived peptide–Human Leukocyte Antigen complex (CMV-pMHC) (CMV-pMHC).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call